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(1,5-Cyclooctadiene)(methoxy)iridium(I) dimer_Molecular_structure_CAS_12148-71-9)
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(1,5-Cyclooctadiene)(methoxy)iridium(I) dimer

Catalog No. 685062 Name Sigma Aldrich
CAS Number 12148-71-9 Website http://www.sigmaaldrich.com
M. F. C18H30Ir2O2 Telephone 1-800-521-8956
M. W. 662.8636 Fax
Purity Email
Storage Chembase ID: 89870

SYNONYMS

Title
甲氧基(环辛二烯)合铱二聚体
IUPAC name
bis(cycloocta-1,5-diene); dimethyl-2,4-dioxa-1,3-diiridabicyclo[1.1.0]butane-2,4-diium-1,3-diuide
IUPAC Traditional name
bis(1,5-cyclooctadiene); dimethyl-2,4-dioxa-1,3-diiridabicyclo[1.1.0]butane-2,4-diium-1,3-diuide
Synonyms
二(1,5-环辛二烯)二-Μ-甲氧基二铱(I)
Bis(1,5-cyclooctadiene)di-μ-methoxydiiridium(I)
[Ir(OMe)(1,5-cod)]2

DATABASE IDS

MDL Number MFCD08459360
CAS Number 12148-71-9

PROPERTIES

Linear Formula [Ir(OCH3)(C8H12)]2
Melting Point 154-179 °C (D)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
250 mg in glass bottle
Application
Catalyst for:
• Preparation of heteroaryl fused indole ring systems as inhibitors of HCV NS5B polymerase1
• Borylation/Suzuki-Miyaura coupling2
• Metalation-Suzuki cross-coupling procedure for the synthesis of biaryls and heterobiaryls3
• Tetraborylation reactions4
• Highly regio- and enantioselective asymmetric hydroboration5
• Ortho-silylation of aryl ketone, benzaldehyde, and benzyl alcohol derivatives via C-H activation6
Citation
A powerful C-H activation catalyst to prepare phenols from arenes7
Description (简体中文)
包装
1 g in glass bottle
250 mg in glass bottle
Application
Catalyst for:
• Preparation of heteroaryl fused indole ring systems as inhibitors of HCV NS5B polymerase1
• Borylation/Suzuki-Miyaura coupling2
• Metalation-Suzuki cross-coupling procedure for the synthesis of biaryls and heterobiaryls3
• Tetraborylation reactions4
• Highly regio- and enantioselective asymmetric hydroboration5
• Ortho-silylation of aryl ketone, benzaldehyde, and benzyl alcohol derivatives via C-H activation6
Citation
一种强效的 C-H 键活化催化剂,可用于由芳烃制备酚。7

REFERENCES